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Platelet Activating Factor Synthesis and Metabolism in Intestinal Ischaemia-Reperfusion Injury

The object of this study was to characterize the synthesis and metabolism of platelet activating factor (PAF) by intestinal mucosa subjected to ischaemia–reperfusion injury. Canine intestinal mucosa produced 16:0-PAF, 18:0-PAF, and high levels of the corresponding lyso- PAF metabolites. Three h of i...

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Detalles Bibliográficos
Autores principales: Mangino, M. J., Murphy, M., Bohrer, A., Turk, J.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365579/
https://www.ncbi.nlm.nih.gov/pubmed/18475586
http://dx.doi.org/10.1155/S0962935194000554
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author Mangino, M. J.
Murphy, M.
Bohrer, A.
Turk, J.
author_facet Mangino, M. J.
Murphy, M.
Bohrer, A.
Turk, J.
author_sort Mangino, M. J.
collection PubMed
description The object of this study was to characterize the synthesis and metabolism of platelet activating factor (PAF) by intestinal mucosa subjected to ischaemia–reperfusion injury. Canine intestinal mucosa produced 16:0-PAF, 18:0-PAF, and high levels of the corresponding lyso- PAF metabolites. Three h of intestinal ischaemia and ischaemia followed by 1 h of reperfusion did not affect the synthesis or metabolism of PAF by intestinal mucosa. Intestinal mucosa elaborated a factor that rapidly hydrolyzes PAF to lyso-PAF. The observed hydrolysis rate was not altered by ischaemia or ischaemia and reperfusion. In conclusion, this study suggests that intestinal mucosa produces PAF and rapidly hydrolyzes PAF. The PAF synthesis and metabolism rates of intestinal mucosa is not altered by ischaemia reperfusion in this model under the imposed conditions.
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spelling pubmed-23655792008-05-12 Platelet Activating Factor Synthesis and Metabolism in Intestinal Ischaemia-Reperfusion Injury Mangino, M. J. Murphy, M. Bohrer, A. Turk, J. Mediators Inflamm Research Article The object of this study was to characterize the synthesis and metabolism of platelet activating factor (PAF) by intestinal mucosa subjected to ischaemia–reperfusion injury. Canine intestinal mucosa produced 16:0-PAF, 18:0-PAF, and high levels of the corresponding lyso- PAF metabolites. Three h of intestinal ischaemia and ischaemia followed by 1 h of reperfusion did not affect the synthesis or metabolism of PAF by intestinal mucosa. Intestinal mucosa elaborated a factor that rapidly hydrolyzes PAF to lyso-PAF. The observed hydrolysis rate was not altered by ischaemia or ischaemia and reperfusion. In conclusion, this study suggests that intestinal mucosa produces PAF and rapidly hydrolyzes PAF. The PAF synthesis and metabolism rates of intestinal mucosa is not altered by ischaemia reperfusion in this model under the imposed conditions. Hindawi Publishing Corporation 1994 /pmc/articles/PMC2365579/ /pubmed/18475586 http://dx.doi.org/10.1155/S0962935194000554 Text en Copyright © 1994 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mangino, M. J.
Murphy, M.
Bohrer, A.
Turk, J.
Platelet Activating Factor Synthesis and Metabolism in Intestinal Ischaemia-Reperfusion Injury
title Platelet Activating Factor Synthesis and Metabolism in Intestinal Ischaemia-Reperfusion Injury
title_full Platelet Activating Factor Synthesis and Metabolism in Intestinal Ischaemia-Reperfusion Injury
title_fullStr Platelet Activating Factor Synthesis and Metabolism in Intestinal Ischaemia-Reperfusion Injury
title_full_unstemmed Platelet Activating Factor Synthesis and Metabolism in Intestinal Ischaemia-Reperfusion Injury
title_short Platelet Activating Factor Synthesis and Metabolism in Intestinal Ischaemia-Reperfusion Injury
title_sort platelet activating factor synthesis and metabolism in intestinal ischaemia-reperfusion injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365579/
https://www.ncbi.nlm.nih.gov/pubmed/18475586
http://dx.doi.org/10.1155/S0962935194000554
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